Evidence map›Paper›PMID 29463044›Full record

ReviewInternational journal of molecular sciences2018

The Role of the Estrogen Pathway in the Tumor Microenvironment.

Natalie J Rothenberger, Ashwin Somasundaram, Laura P Stabile

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

118 citing papers in PubMed, 1 synthesis or guideline pooled it, 188 citations in OpenAlex.

  1. Pooled it
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  16. Differentiation and mitochondrial metabolic characteristics of CD8Cancer immunology, immunotherapy : CII · 2025
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58 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Natalie J RothenbergerDepartment of Medicine, Division of Hematology/Oncology, University of Pittsburgh, Pittsburgh, PA 15232, USA. njr31@pitt.edu.
Ashwin SomasundaramDepartment of Medicine, Division of Hematology/Oncology, University of Pittsburgh, Pittsburgh, PA 15232, USA. somasundarama@upmc.edu.
Laura P StabileDepartment of Pharmacology & Chemical Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA. stabilela@upmc.edu.
University of Pittsburgh · USUPMC Hillman Cancer Center · US

Funding

Vitamin D3 Modulation of Inflammation and Lung Cancer RiskP50CA090440 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SIEGFRIED, JILL M · 2001 to 2015
$34.6M
Training in Cancer Therapeutics ResearchT32CA193205 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BUCKANOVICH, RONALD J · 2015 to 2019
$893k
NCI NIH HHS P50 CA090440NCI NIH HHS T32 CA193205
6 · The paper itself

Abstract

Estrogen receptors are broadly expressed in many cell types involved in the innate and adaptive immune responses, and differentially regulate the production of cytokines. While both genomic and non-genomic tumor cell promoting mechanisms of estrogen signaling are well characterized in multiple carcinomas including breast, ovarian, and lung, recent investigations have identified a potential immune regulatory role of estrogens in the tumor microenvironment. Tumor immune tolerance is a well-established mediator of oncogenesis, with increasing evidence indicating the importance of the immune response in tumor progression. Immune-based therapies such as antibodies that block checkpoint signals have emerged as exciting therapeutic approaches for cancer treatment, offering durable remissions and prolonged survival. However, only a subset of patients demonstrate clinical response to these agents, prompting efforts to elucidate additional immunosuppressive mechanisms within the tumor microenvironment. Evidence drawn from multiple cancer types, including carcinomas traditionally classified as non-immunogenic, implicate estrogen as a potential mediator of immunosuppression through modulation of protumor responses independent of direct activity on tumor cells. Herein, we review the interplay between estrogen and the tumor microenvironment and the clinical implications of endocrine therapy as a novel treatment strategy within immuno-oncology.

Indexed as

EstrogensHumansImmunotherapyNeoplasmsReceptors, EstrogenSignal TransductionTumor MicroenvironmentEstrogensReceptors, Estrogencancerestrogenimmunosuppressionimmunotherapytumor microenvironment

Identifiers

PMID29463044
PMCPMC5855833
OpenAlexW2789622120

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.